IT Validation Specialist (CSV)

IT Validation Specialist (CSV)

Contract Type:

Contractor

Location:

Durham - North Carolina

Industry:

Technology

Reference Number:

CR/509844

Salary:

$60 - $70 Hourly

Contact Name:

Tandym Group

Contact Email:

stuart.schwartz@tandymgroup.com

Contact Phone:


Date Published:

04-Mar-2026

A biotech company is seeking a new IT Validation Specialist (CSV) on a long-term contract basis in a Remote capacity.

*** Third-party candidates will NOT BE CONSIDERED! Only direct candidates.***

About the Opportunity:
  • Schedule: Monday to Friday
  • Hours: 9am to 5pm (40 hours per week)
  • Setting: Remote
Responsibilities:
  • Execute the GxP-Regulated computerized system lifecycle, ensuring compliance with regulatory standards, CSV procedures, and Data Integrity requirements
  • Manage and execute all CSV/CSA activities at the site, ensuring compliance with regulatory requirements and internal SOPs
  • Plan, organize, and lead the development and execution of all validation lifecycle documents, including:
  • Validation Plan
  • Requirements Specification
  • Risk Assessment
  • System Impact Assessment
  • Testing Documentation
  • Requirements Traceability Matrix
  • Validation Final Report
  • Work closely with project teams, business partners, and Digital Quality to determine scope of validation activities
  • Conduct periodic reviews of validated computerized systems to ensure continued compliance with regulations and SOPs
  • Participate in change management activities for validated computerized systems as a subject matter expert, including providing thorough impact assessments of proposed changes to ensure no negative impact on system integrity or data compliance
  • Providing support during regulatory and external audits, serving as a subject matter expert for CSV/CSA
Qualifications:
  • 4+ years of experience in Computer Systems Validation/Assurance
  • Detailed knowledge of GxP regulations and CSV/CSA principles, including, but not limited to: 21 CFR Part 11, Annex 11, GAMP 5, and Data Integrity
  • Familiarity with manufacturing computerized systems, including but not limited to:
  • Clinical applications like EDS, cTMS, eTMF
  • Commercial pharma analytics systems
  • IT CSV and Quality control applications
  • Data Backup/Restore Solutions
  • Asset Management Systems
  • Excellent communication and interpersonal skills, fostering collaboration and building strong relationships with internal and external stakeholders
  • Project management skills with the ability to prioritize tasks, manage deadlines, and track progress effectively
  • Strong attention to detail and a commitment to accuracy and compliance
APPLY NOW

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